Papers associated with primary germ layer (and pax8)

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	In vitro modeling of cranial placode differentiation: Recent advances, challenges, and perspectives., Griffin C., Dev Biol. February 1, 2024; 506 20-30.
	Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ., J Exp Zool B Mol Dev Evol. October 13, 2023;
	Xenopus Ssbp2 is required for embryonic pronephros morphogenesis and terminal differentiation., Cervino AS., Sci Rep. October 4, 2023; 13 (1): 16671.
	Retinoic acid control of pax8 during renal specification of Xenopus pronephros involves hox and meis3., Durant-Vesga J., Dev Biol. January 1, 2023; 493 17-28.
	Alcohol induces neural tube defects by reducing retinoic acid signaling and promoting neural plate expansion., Edri T., Front Cell Dev Biol. January 1, 2023; 11 1282273.
	Hnf1b renal expression directed by a distal enhancer responsive to Pax8., Goea L., Sci Rep. November 19, 2022; 12 (1): 19921.
	The enpp4 ectonucleotidase regulates kidney patterning signalling networks in Xenopus embryos., Massé K., Commun Biol. October 7, 2021; 4 (1): 1158.
	Molecular mechanisms of hearing loss in Nager syndrome., Maharana SK., Dev Biol. August 1, 2021; 476 200-208.
	A Critical E-box in Barhl1 3' Enhancer Is Essential for Auditory Hair Cell Differentiation., Hou K., Cells. May 15, 2019; 8 (5):
	Arid3a regulates nephric tubule regeneration via evolutionarily conserved regeneration signal-response enhancers., Suzuki N., Elife. January 8, 2019; 8
	Characterization of potential TRPP2 regulating proteins in early Xenopus embryos., Futel M., J Cell Biochem. December 1, 2018; 119 (12): 10338-10350.
	The Lhx1-Ldb1 complex interacts with Furry to regulate microRNA expression during pronephric kidney development., Espiritu EB., Sci Rep. October 30, 2018; 8 (1): 16029.
	Fam46a regulates BMP-dependent pre-placodal ectoderm differentiation in Xenopus., Watanabe T., Development. October 26, 2018; 145 (20):
	Anosmin-1 is essential for neural crest and cranial placodes formation in Xenopus., Bae CJ., Biochem Biophys Res Commun. January 15, 2018; 495 (3): 2257-2263.
	Pou3f transcription factor expression during embryonic development highlights distinct pou3f3 and pou3f4 localization in the Xenopus laevis kidney., Cosse-Etchepare C., Int J Dev Biol. January 1, 2018; 62 (4-5): 325-333.
	Peroxiredoxin1, a novel regulator of pronephros development, influences retinoic acid and Wnt signaling by controlling ROS levels., Chae S., Sci Rep. August 21, 2017; 7 (1): 8874.
	Pax2/Pax8-defined subdomains and the occurrence of apoptosis in the posterior placodal area of mice., Washausen S., Brain Struct Funct. August 1, 2017; 222 (6): 2671-2695.
	pdzrn3 is required for pronephros morphogenesis in Xenopus laevis., Marracci S., Int J Dev Biol. January 1, 2016; 60 (1-3): 57-63.
	Hspa9 is required for pronephros specification and formation in Xenopus laevis., Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.
	Cooperative and independent functions of FGF and Wnt signaling during early inner ear development., Wright KD., BMC Dev Biol. October 6, 2015; 15 33.
	Transcriptional regulator PRDM12 is essential for human pain perception., Chen YC, Chen YC., Nat Genet. July 1, 2015; 47 (7): 803-8.
	TRPP2-dependent Ca2+ signaling in dorso-lateral mesoderm is required for kidney field establishment in Xenopus., Futel M., J Cell Sci. March 1, 2015; 128 (5): 888-99.
	Pax8 and Pax2 are specifically required at different steps of Xenopus pronephros development., Buisson I., Dev Biol. January 15, 2015; 397 (2): 175-90.
	Understanding early organogenesis using a simplified in situ hybridization protocol in Xenopus., Deimling SJ., J Vis Exp. January 12, 2015; (95): e51526.
	Specific induction of cranial placode cells from Xenopus ectoderm by modulating the levels of BMP, Wnt and FGF signaling., Watanabe T., Genesis. October 1, 2014; .
	The evolutionary history of vertebrate cranial placodes--I: cell type evolution., Patthey C., Dev Biol. May 1, 2014; 389 (1): 82-97.
	The evolutionary history of vertebrate cranial placodes II. Evolution of ectodermal patterning., Schlosser G., Dev Biol. May 1, 2014; 389 (1): 98-119.
	Differential expression of arid5b isoforms in Xenopus laevis pronephros., Le Bouffant R., Int J Dev Biol. January 1, 2014; 58 (5): 363-8.
	Comparative Functional Analysis of ZFP36 Genes during Xenopus Development., Tréguer K., PLoS One. January 1, 2013; 8 (1): e54550.
	Retinoic acid-dependent control of MAP kinase phosphatase-3 is necessary for early kidney development in Xenopus., Le Bouffant R., Biol Cell. September 1, 2012; 104 (9): 516-32.
	Suppression of Bmp4 signaling by the zinc-finger repressors Osr1 and Osr2 is required for Wnt/β-catenin-mediated lung specification in Xenopus., Rankin SA, Rankin SA., Development. August 1, 2012; 139 (16): 3010-20.
	Mutual repression between Gbx2 and Otx2 in sensory placodes reveals a general mechanism for ectodermal patterning., Steventon B., Dev Biol. July 1, 2012; 367 (1): 55-65.
	Evolution of a tissue-specific silencer underlies divergence in the expression of pax2 and pax8 paralogues., Ochi H., Nat Commun. May 22, 2012; 3 848.
	Myogenic waves and myogenic programs during Xenopus embryonic myogenesis., Della Gaspera B., Dev Dyn. May 1, 2012; 241 (5): 995-1007.
	Differential distribution of competence for panplacodal and neural crest induction to non-neural and neural ectoderm., Pieper M., Development. March 1, 2012; 139 (6): 1175-87.
	Xenopus as a model system for the study of GOLPH2/GP73 function: Xenopus GOLPH2 is required for pronephros development., Li L., PLoS One. January 1, 2012; 7 (6): e38939.
	Origin and segregation of cranial placodes in Xenopus laevis., Pieper M., Dev Biol. December 15, 2011; 360 (2): 257-75.
	V-ATPase-dependent ectodermal voltage and pH regionalization are required for craniofacial morphogenesis., Vandenberg LN., Dev Dyn. August 1, 2011; 240 (8): 1889-904.
	Lhx1 is required for specification of the renal progenitor cell field., Cirio MC., PLoS One. April 15, 2011; 6 (4): e18858.
	Use of fully modified 2'-O-methyl antisense oligos for loss-of-function studies in vertebrate embryos., Schneider PN., Genesis. March 1, 2011; 49 (3): 117-23.
	The nephrogenic potential of the transcription factors osr1, osr2, hnf1b, lhx1 and pax8 assessed in Xenopus animal caps., Drews C., BMC Dev Biol. January 31, 2011; 11 5.
	Retinoic acid is a key regulatory switch determining the difference between lung and thyroid fates in Xenopus laevis., Wang JH., BMC Dev Biol. January 26, 2011; 11 75.
	The secreted integrin ligand nephronectin is necessary for forelimb formation in Xenopus tropicalis., Abu-Daya A., Dev Biol. January 15, 2011; 349 (2): 204-12.
	Inversin relays Frizzled-8 signals to promote proximal pronephros development., Lienkamp S., Proc Natl Acad Sci U S A. November 23, 2010; 107 (47): 20388-93.
	XPteg (Xenopus proximal tubules-expressed gene) is essential for pronephric mesoderm specification and tubulogenesis., Lee SJ., Mech Dev. January 1, 2010; 127 (1-2): 49-61.
	The miR-30 miRNA family regulates Xenopus pronephros development and targets the transcription factor Xlim1/Lhx1., Agrawal R., Development. December 1, 2009; 136 (23): 3927-36.
	Coordinating the timing of cardiac precursor development during gastrulation: a new role for Notch signaling., Miazga CM., Dev Biol. September 15, 2009; 333 (2): 285-96.
	In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
	Requirement of Wnt/beta-catenin signaling in pronephric kidney development., Lyons JP., Mech Dev. January 1, 2009; 126 (3-4): 142-59.
	Hindbrain-derived Wnt and Fgf signals cooperate to specify the otic placode in Xenopus., Park BY., Dev Biol. December 1, 2008; 324 (1): 108-21.

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